|Publication number||US8071388 B2|
|Application number||US 12/391,898|
|Publication date||Dec 6, 2011|
|Filing date||Feb 24, 2009|
|Priority date||Sep 28, 2006|
|Also published as||CA2664649A1, EP2066813A2, US20090275142, WO2008054600A2, WO2008054600A3|
|Publication number||12391898, 391898, US 8071388 B2, US 8071388B2, US-B2-8071388, US8071388 B2, US8071388B2|
|Inventors||Yumei Huang, James M. Coull|
|Original Assignee||Ensemble Therapeutics Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (26), Non-Patent Citations (23), Referenced by (1), Classifications (35), Legal Events (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation-in-part of International Patent Application Serial No. PCT/US2007/021094, filed Sep. 28, 2007, which claims the benefit of and priority to U.S. patent application Ser. Nos. 60/847,859, filed Sep. 28, 2006; 60/905,364, filed Mar. 7, 2007; and 60/918,023, filed Mar. 14, 2007; and International Patent Application Serial No. PCT/US2007/021094 is a continuation-in-part of International Patent Application Serial No. PCT/US2007/020223, filed Sep. 18, 2007, the entire disclosure of each of which is incorporated by reference herein for all purposes.
The present invention relates generally to probes and their use in biodetection and diagnostics. More particularly, the invention relates to compositions and methods for biodetection using nucleic acid-templated chemistry (e.g., synthesis of compounds having desired fluorescent, chemiluminescent or chromophoric properties in a multiplex detection of nucleic acids or proteins).
Fluorescent and colored compounds have been used in the fields of biological research and medicine to detect the presence, absence, state, quantity, and composition of biomolecules. Assays using fluorescent and colored compounds may be performed in vitro, in situ, or in vivo. Examples of commonly used in vitro assays for detection of DNA and RNA are real-time and end-point polymerase chain reaction (PCR), DNA sequencing, and DNA microarray technologies.
Recently, there has been an increased amount of literature published on detection methods for multiple analytes, most of which involves genetic analysis and some relates to protein detection. See, e.g., U.S. Pat. No. 6,890,741.
In a typical nucleic acid detection method used for diagnostic and molecular biology research, multiple gene probes complementary with a gene of interest are labeled with small molecules that can be detected by spectroscopic, electrochemical, biochemical or immunochemical means. PCR is generally incorporated for the amplification of targeted gene sequences. To achieve detection of multiple analytes, fluorescence-based technologies have been used often due to fluorescence dyes readily available. For example, primers have been labeled with different fluorescence dyes and the changes in fluorescence were monitored upon hybridization to their complements (e.g., WO 2002/057479). In other cases, the multiplex detection was achieved by using intercalating dyes as labels in DNA restriction fragment analysis and capillary electrophoresis with frequency-domain fluorescence lifetime detection method (McIntosh, et al., Electrophoresis, 2002, 23, 1473-1479). Since these methods use pre-labeled fluorescence dyes, the detection sensitivity relies largely on the separation of target bound and unbound fluorescence labeled probes. Though solid phase immobilization of the target gene (fluorescence in situ hybridization, for example) can improve the separation efficiency by simply washing away the unbound fluorescence labeled probes, this introduces an extra process. However, the potential background still can be high, and the procedure can be laborious. To address this problem, a non-fluorescence label moiety can be attached to the probes so that the fluorescence signal only occurs after the hybridization event. Recently, the development of DNA-programmed chemistry has provided a novel approach for generation of fluorescence dye in situ. See, e.g., Li, X.; Liu, D. R. Angew. Chem. Int. Ed. 2004, 43, 4848-4870; U.S. Pat. No. 7,070,928.
Polymethine dye has been widely used as laser dyes, photographic sensitizers and fluorescence probes due to its superior fluorescence and photochemical properties. However, polymethine dyes are generally synthesized by acid/base catalyzed condensation under anhydrous conditions which is not comparable to the nucleic acid-templated chemistry (Jedrzejewska, et al. Dyes and Pigments 2003, 58, 47-58). Recently, the literature has reported an improved aldol condensation in water using Lewis-acid (Kobayashi, et al., J. Am. Chem. Soc. 1998, 120, 8287-8288) and enamine-based organocatalyst (Mase, et al. J. Am. Chem. Soc. 2006, 128, 734-735). The quaternary salt of polymethine precursor (active hydrogen component) used for condensing with aldehyde, however, is different substantially from the precursor (alpha carbon of aldehyde) in a conventional aldol condensation.
Thus, there exists a need for new fluorescent and colorimetric technologies that address many of the shortcomings inherent in the above-mentioned biodetection methods. For example, there is a need for methods of polymethine dye synthesis from non-detectable precursors by nucleic acid-templated chemistry and adaptation of such chemistry to biodetection.
The present invention is based, in part, upon the discovery that nucleic acid-templated chemistry can be applied in detection of multiple biological targets simultaneously. The present invention is based, in part, upon the discovery that polymethine dyes can be synthesized by nucleic acid-templated chemistry. Assays of this invention may be performed in vitro, in situ, or in vivo.
In one aspect, the present invention relates to a method for making a polymethine dye comprising conducting an aldol condensation between an aldehyde and an active hydrogen component in an aqueous condition in the presence of an organocatalyst.
In some embodiments, the condensation reaction is:
and wherein the organocatalyst is a secondary amine, a primary amine, a bifunctional amine-acid catalyst or a diamine. The secondary amine may be a pyrrolidine, a piperidine, a nornicotine, or an analog thereof, for example. The primary amine may be a valine or a peptide having fewer than 3 amino acid units, for example. The bifunctional amine-acid catalyst may be pyrrolidine/AcOH, for example. The diamine catalyst may be N1,N1-dimethylethane-1,2-diamine, propane-1,2-diamine, 1-(2-aminoethyl)-piperidine, or an analog thereof, for example.
In some embodiments, the organocatalyst is represented by:
wherein each R is independently selected from hydrogen or C1-C6 straight or branched alkyl.
In another aspect, the invention generally relates to a hemicyanine dye having the chemical structure of (I), (II) or (III), for example, prepared by the methods disclosed herein.
In yet another aspect, the invention generally relates to an aldehyde having the chemical structure of IV or V:
In yet another aspect, the invention generally relates to a quaternary salt having the chemical structure of VI or VII:
In yet another aspect, the invention generally relates to an quaternary salt-nucleic acid conjugate having the chemical structure of:
In yet another aspect, the invention generally relates to an aldehyde-nucleic acid conjugate having the chemical structure of:
In yet another aspect, the invention generally relates to a hemicyanine dye-nucleic acid conjugate having the chemical structure of:
In yet another aspect, the invention generally relates to making a hemicyanine-nucleic acid conjugate comprising conducting a nucleic acid-templated reaction between an aldehyde and quaternary salt disclosed herein to make a hemicyanine disclosed herein.
In some embodiments, the nucleic acid-templated reaction is in an end of helix architect. In some other embodiments, the nucleic acid-templated reaction is in a middle of helix architect.
In yet another aspect, the invention generally relates to a method for selecting a dye having a desired fluorescent property. The method includes (a) preparing a library of oligonucleotide-encoded dyes through nucleic acid-templated synthesis; (b) hybridizing the oligonucleotide-encoded dyes with spatially arrayed complementary oligonucleotide probes immobilized on a solid support; (c) measuring the absorption and fluorescence properties of the oligonucleotide-encoded dye directly on the solid support; (d) identifying the oligonucleotides that encode the dyes having the desired fluorescence properties based on the position of the immobilized complementary oligonucleotide probes, and (e) identifying and characterizing the chemical structure of the dyes having the desired fluorescence property.
In yet another aspect, the invention generally relates to a method for detecting multiple target nucleotide sequences. The method includes: (a) providing a number of probe pairs, the number equal to the number of target nucleotide sequences, wherein each probe pair comprises (1) a first probe comprising (i) a first oligonucleotide sequence and (ii) a first reactive group linked to the first oligonucleotide sequence, and (2) a corresponding second probe comprising (i) a second oligonucleotide sequence and (ii) a second reactive group linked to the second oligonucleotide sequence, wherein the first oligonucleotide sequence and the second oligonucleotide sequence are complementary to two separate regions of a corresponding target nucleotide sequence; (b) combining the probe pairs with a sample to be tested for the presence of the target nucleotide sequences under conditions where the first probes and the second probes hybridize to their respective complementary regions of the target nucleotide sequences if present in the sample thereby bringing into reactive proximity the first reactive groups and the corresponding second reactive groups; and (c) detecting one or more reactions between the first reactive groups and the corresponding second reactive groups thereby determining the presence of the target nucleotide sequences.
The number of target nucleotide sequences may be between about 2 to about 20, for example, 2 to 6. The target nucleotide sequences may be in solution phase. The target nucleotide sequences may be attached to a solid support. In some embodiments, the one or more reactions between the first reactive groups and the corresponding second reactive groups generate fluorescent compounds that may be detected. In some embodiment, the one or more reactions between the first reactive groups and the corresponding second reactive groups generate chemiluminescent compounds that may be detected.
The one or more reactions between the first reactive groups and the corresponding second reactive groups may comprise an aldol condensation reaction, for example. The one or more reactions between the first reactive groups and the corresponding second reactive groups may comprise a Wittig reaction.
The invention encompasses a kit that provides one, two or more of the probes described herein. More particularly, the invention encompasses a kit that provides one, two or more of the probes that utilize nucleic acid-templated chemistry for the generation of detectable signals as a way for detecting the presence of biological targets.
The foregoing aspects and embodiments of the invention may be more fully understood by reference to the following figures, detailed description and claims.
The term, “DNA programmed chemistry” or “DPC”, as used herein, refers to nucleic acid-templated chemistry, for example, sequence specific control of chemical reactants to yield specific products accomplished by (1) providing one or more templates, which have associated reactive group(s); (2) contacting one or more transfer groups (reagents) having an anti-codon (e.g., complementary sequence with one or more templates) and reactive group(s) under conditions to allow for hybridization to the templates and (3) reaction of the reactive groups to yield products. For example, in a one-step nucleic acid-templated reaction, hybridization of a “template” and a “complementary” oligonucleotide bring together reactive groups followed by a chemical reaction that results in the desired product. Structures of the reactants and products need not be related to those of the nucleic acids comprising the template and transfer group oligonucleotides. See, e.g., U.S. Pat. No. 7,070,928 and U.S. Application Publication No. 2004/0180412 A1, by Liu et al.; Gartner, et al., 2004, Science, vol. 305, pp. 1601-1605; Doyon, et al., 2003, JACS, vol. 125, pp. 12372-12373, all of which are expressly incorporated herein by reference in their entireties. See, also, “Turn Over Probes and Use Thereof” by Coull et al., PCT International Patent Application PCT/US06/16999, filed on May 3, 2006; U.S. patent application Ser. No. 11/441,804, “Biodetection by Nucleic Acid-Templated Chemistry” by Coull et al., filed on May 26, 2006.
The terms, “nucleic acid”, “oligonucleotide” (sometimes simply referred to as “oligo”) or “polynucleotide” or as used herein refer to a polymer of nucleotides. The polymer may include, without limitation, natural nucleosides (i.e., adenosine, thymidine, guanosine, cytidine, uridine, deoxyadenosine, deoxythymidine, deoxyguanosine, and deoxycytidine), nucleoside analogs (e.g., 2-aminoadenosine, 2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyl adenosine, 5-methylcytidine, C5-bromouridine, C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine, C5-propynyl-cytidine, C5-methylcytidine, 7-deazaadeno sine, 7-deazaguano sine, 8-oxoadenosine, 8-oxoguanosine, O(6)-methylguanine, and 2-thiocytidine), chemically modified bases, biologically modified bases (e.g., methylated bases), intercalated bases, modified sugars (e.g., 2′-fluororibose, ribose, 2′-deoxyribose, arabinose, and hexose), or modified phosphate groups (e.g., phosphorothioates and 5′-N-phosphoramidite linkages). Nucleic acids and oligonucleotides may also include other polymers of bases having a modified backbone, such as a locked nucleic acid (LNA), a peptide nucleic acid (PNA), a threose nucleic acid (TNA).
Throughout the description, where compositions are described as having, including, or comprising specific components, or where processes are described as having, including, or comprising specific process steps, it is contemplated that compositions of the present invention also consist essentially of, or consist of, the recited components, and that the processes of the present invention also consist essentially of, or consist of, the recited processing steps. Further, it should be understood that the order of steps or order for performing certain actions are immaterial so long as the invention remains operable. Moreover, two or more steps or actions may be conducted simultaneously.
The invention may be further understood from the following figures in which:
In its simplest sense, the invention is to detect the presence of target analytes via nucleic acid-templated chemistry, for example, through measurement of fluorescence of polymethine dyes generated by nucleic acid-templated reactions templated by target nucleic acids or proteins. The present invention provides methods for analysis of multiple analytes in a convenient, accurate and sensitive way. For example, in the detection of nucleic acids, the method uses nucleic acid probes conjugated with non-fluorescence precursor (e.g., aldehydes and methyl quaternary salts) and polymethine multiplex dyes are generated through the chemical reaction of the probes upon hybridization with target nucleic acids. In addition, the invention provides novel chemical compositions of polymethine dyes and methods of synthesizing polymethine dyes in conventional reactions under aqueous conditions as well as via nucleic acid-templated chemistry.
Polymethine Dye Chemistry
Polymethine dye is characterized by a chain of methine (—CH═) groups with an electron donor (D) and an electron acceptor (A) at opposite ends of their polyene chain (
Scheme 1 depicts hemicyanine formation through organocatalytic aldol condensation in aqueous buffer. Some of the general organocatalysts such as pyrrolidine analogues have been listed here. By using catalyst, the reaction condition for the hemicyanine formation can switch from anhydrous to aqueous condition. The percentage of the water content used depends only on the solubility of the starting materials.
Scheme 2 is a schematic illustration of hemicyanine dye generation through DPC in the presence of organocatalyst. The general chemical structures of component A (aldehyde_DNA), component B (quaternary salt bearing active hydrogen component) and hemicyaine_DNA conjugate have also been described. The fluorescence emission wavelength of the hemicyaine dye can be tuned by changing the number of the vinyl group in the polyene chain (n) or by using different substitute groups (R′) and terminal groups in component B.
There are a number of advantages to the detection methods disclosed here. 1) Zero background. There is no background fluorescence signal for aldehyde and quaternary salt precursors when excited at the polymethine product's excitation wavelength. Since the DPC reaction only happens in the presence of the catalyst and the aldehyde and quaternary salt precursors are very stable, no decomposition of precursors will be observed and thus there is no background fluorescence of the decomposed product. 2) Simplicity. The fluorescence generation is performed in one-pot and the detection is achieved in situ without isolation of the product. 3) Specificity. The fluorescence generation is based on the sequence specific nucleic acid interaction, so the signal generation is specific to the nucleic acid sequence. 4) A larger number of analytes can be detected as compared to conventional methods. The fluorescence emission wavelength of polymethine dye can be easily tuned from far UV to near IR, so multi-wavelength dyes can be generated in one-pot by utilizing multi-codon DNAs. The numbers of analyte that can be detected are not limited by the DPC and dye chemistry.
Various and general aspects of nucleic acid-templated chemistry are discussed in detail below. Additional information may be found in U.S. Pat. Nos. 7,070,928, and 7,223,545, European Patent No. 1,423,400 B1 and U.S. Application Publication No. 2004/0180412 A1 (U.S. Ser. No. 10/643,752) by Liu et al. Gartner, et al., 2004, Science, vol. 305, pp. 1601-1605; Doyon, et al., 2003, JACS, vol. 125, pp. 12372-12373, all of which are expressly incorporated herein by reference in their entireties. See, also, “Turn Over Probes and Use Thereof” by Coull et al., PCT WO07/008,276A2, filed on May 3, 2006.
DPC-Based Protein Detection
Methods and compositions of biodetection using nucleic acid-templated chemistry based probes are described in WO06128138A2 by Coull et al., which is incorporated herein by reference in its entirety.
More particularly illustrated in
The prefluorophores may reside in an “end of helix” configuration (
The proximity effect afforded by tethering the pair of oligonucleotides may affect the kinetics of annealing of two complementary oligonucleotide sequences compared to the two oligonucleotides free in solution. More importantly, a localized high concentration shifts the melting curve upwards compared to the free complex, i.e. increase the Tm of the complex. In a bulk solution, it is known that Tm has dependence upon total oligonucleotide concentration as illustrated in the equation below. Wetmur, Criti. Rev. in Biochem. And Mol. Biol., 1991, 26, 227-259.
T m=(1000*ΔH)/(A+ΔS+R ln(C t/4)−273.15+16.6 log Na+)
where ΔH and ΔS are the enthalpy and entropy for helix formation, R is the molar gas constant, Ct is the total concentration of oligomers, and Na+ is the molar concentration of sodium ion in the solution.
Reaction products of R1 and R2 may be released from the hybridization complex as a result of the chemical transformation. Thus, the fluorophore or chromophore may be separated from the hybridization complex and analyzed independently, or the fluorophore or chromophore and the annealed oligonucleotides may be removed once detected so that additional rounds of interrogation of the sample can be conducted. The reaction between R1 and R2 may or may not be covalently linked to the two probes once the product(s) is formed.
This zip-coded architecture supports creating a single reporter-oligonucleotide conjugate which would assemble with different downstream reporter oligonucleotides through an anti-zip code sequence. Libraries of different reporters linked to a unique anti-zip code may be tested simply by mixing each one with stoicheometric amounts of the binder-zip code oligonucleotide conjugate with its complementary zip code.
One advantage of the “zip coded” approach is the ability to create the reporter oligonucleotides separately, and have them assemble together with binders under conditions retaining the activities of both the binders and of the nucleic acid template-activated chemistry.
The zip-coded system is based upon two pairs of oligonucleotides, with each pair being held together by the base-pairing of a unique zip code and an anti-zip code pair. “Zip codes” are oligonucleotide sequences which bind specifically to their complementary sequences, and preferably are designed such they are not complementary to known genomic sequences (relevant if the sample may contain genomic DNA), have similar Tm values, lack significant secondary structure, and do not anneal to other zip code or anti-zip code sequences in the detection system.
It is worth pointing out the methods of the invention do not require enzymatic or chemical ligation of the first and/or the second oligonucleotide sequences.
Factors that may be considered in optimizing a design of a zip-coded architecture include, for example, (1) spacer groups (e.g., oligonucleotides and/or non-base groups) between the aptamer/antibody and zip codes (spacer 1), e.g., to allow hybridization partners to reach each other, to prevent any steric hindrance; (2) Length of a zip code sequence in order to form a sufficiently stable annealing to the anti-zip code sequence to form the complex; and (3) Spacer groups (spacer 2) between the anti-zip code and the reporter sequence, e.g., to prevent any steric hindrance.
The binders (target binding moieties) attached to the oligonucleotides may be any chemical moieties that specifically bind to a target molecule and allow the design of the invention to work. Examples include a wide range of functionalities, such as (1) antibodies: e.g., IgG, IgM, IgA, IgE, Fab's, Fab′, F(ab)2, Dab, Fv or ScFv fragments; (2) small molecule binders, such as inhibitors, drugs, cofactors; (3) receptors for protein detection, and vice versa; (4) DNA, RNA, PNA aptamers; (5) DNA sequences for DNA-binding and regulatory proteins; (6) peptides representing protein binding motifs; (7) peptides discovered through phage display, random synthesis, mutagenesis; (8) naturally binding protein pairs and complexes; (9) antigens (for antibody detection); and (10) a single polyclonal antibody separately attached to two oligonucleotides may serve as two separate binders of different specificity.
The target binding moieties attached to the oligonucleotides may be of heterogeneous types directed against different sites within the same target. For example, the two binders may be two different antibodies, an antibody and a receptor, an antibody and a small molecule binder, a receptor and a peptide, an aptamer and a cofactor, or any other combination.
The target analytes can be of any type, provided the target supports two (or more) binding sites. Molecules which exist in equilibrium with a monomeric form and a homodimeric or higher polymerization phase may be detected by a pair of probes containing the same binder but different complementary DNA sequences. Suitable targets include proteins, cell surfaces, antibodies, antigens, viruses, bacteria, organic surfaces, membranes, organelles, in situ analysis of fixed cells, protein complexes. The invention may be particularly suited for the detection of fusion proteins (e.g., BCR-ABL in the presence of BCR and ABL).
In the design of the probes, one consideration is the Tm of the two reporter sequences carrying the reactive groups. Since the Tm of the duplex should be below room temperature in the absence of a target, this sequence normally should be short, for example 6-15 bases and/or A-T rich. A typical reporter length of 10 base pairs might have a Tm of around 30° C. at a low salt concentration. Therefore, it is often necessary even with a short sequence to add 10% to 40% volume/volume formamide to further lower the temperature below assay temperature, or to elevate the assay temperature. Very short reporter oligonucleotides may suffer from a lack of specificity and exhibit some binding to zip code sequences (when these are employed) which is undesirable.
Another factor in the design of the probes is the length of oligonucleotide in between the binding moiety and the reporter sequence, including any zip code sequences. These must be long enough for the reporter oligonucleotides to reach each other and anneal. The sequences may be interspersed with polyethylene glycol (PEG) linkers that are flexible and may afford additional protection against any steric hindrance. For example, total lengths of oligonucleotides may be around 35 bases long. Oligonucleotides containing 0, 1, or 2 C18 PEG spacers, or homopolymer tracts may also be utilized (i.e. C10).
A third consideration is the length of zip and anti-zip sequences when these are employed (i.e.
Regarding signal generation, nucleic acid-templated chemistry may be used to create or destroy a label that effects an optical signal, e.g., creating or destroying a fluorescent, chemiluminescent, or colorimetric molecule. Additionally, a detection reaction may be designed to create or destroy a product that directly or indirectly creates a detectable label, for example, a product that catalyzes a reaction that creates an optical label; inhibits a reaction that creates an optical label; is a fluorescence quencher; is a fluorescent energy transfer molecule; creates a Ramen label; creates an electrochemiluminescent label (i.e. ruthernium bipyridyl); produces an electron spin label molecule.
The following examples contain important additional information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof. Practice of the invention will be more fully understood from these following examples, which are presented herein for illustrative purpose only, and should not be construed as limiting in anyway.
Examples 1 to 4 are related to DNA probe preparation. Both the aldehyde and heterocyclic precursors bearing an active hydrogen component can be conjugated to DNA through amide bond formation. First, an acid heterocyclic or aromatic precursor is synthesized. The acid is then converted to the active N-hydroxysuccimide ester (NHS ester) that readily reacts with DNA bearing amine functionality.
Oligonucleotides were prepared using standard phosphoramidite chemistry and purified by reversed-phase C18 column (Glen Research, Sterling Va., USA). Oligonucleotides bearing 5′-amino groups were prepared using 5′-Amino-Modifier 5 and oligonucleotides bearing 3′-aminogroups were prepared using 3′-Amino-Modifier C7 CPG (Glen Research, Sterling Va., USA). Concentration of the DNA and heterocyclic conjugated DNA was determined by UV absorbance at 260 nm. The contribution of the UV absorbance at 260 nm from the heterocyclic moiety in the heterocyclic conjugated DNA was negligible and was not considered.
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X = Spacer Phosphoramidite 18 (Glen Research, Sterling VA, USA)
Scheme 3 gives one example of synthesizing DNA conjugated quaternary salt bearing active hydrogen component (indolinium_DNA). 2,3,3-trimethylindolenine is commercially available. The acid functionality is introduced to the indoline ring through N-quaternization.
Synthesis of compound 1: To 5-bromovaleric acid (2.435 g, 13.45 mmole) was added 2,3,3-trimethylindolenine (2.141 g, 13.45 mmole). The reaction mixture was heated with rigorous stirring at 110° C. overnight. The dark red sticky oil obtained was transferred to a Gregar extractor and extracted with EtOAc overnight. A light red solid was obtained. The solid was redissolved in 30 mL of MeOH. MeOH was removed under reduced pressure and the remaining residue was treated with 10 mL of EtOAc. Brownish solid was precipitated out and filtrated. The solid was washed with 2×50 mL of acetone and 2×100 mL of EtOAc. Total 1.590 g of light brownish solid was obtained (35% yield). 1H NMR (DMSO) δppm: 7.98 (m, 1H), 7.84 (m, 1H), 7.61 (m, 2H), 4.49 (t, 2H), 2.84 (s, 3H), 2.30 (t, 2H), 1.84 (m, 2H), 1.63 (m, 2H), 1.53 (s, 6H). MALDI-MS (positive mode): 260.2419.
Synthesis of compound 2: Compound 1 (0.1 g, 0.294 mmole), N-hydroxy succimide (0.068 g, 0.588 mmole) and N,N′-dicyclohexylcarbodiimide (DCC) (0.085 g, 0.411 mmole) were dissolved in 1.5 mL of dimethyl formamide (DMF). The reaction mixture was stirred at 37° C. for 1 hr. The precipitated dicyclohexylurea (DCU) was removed by filtration, and the filtrate was treated with 15 mL of ether. Light orange solid was washed three times with 10 mL of ether and dried under vacuum for several hours. The solid obtained was used directly for the next reaction. MALDI-MS (positive mode): 357.1590.
Labeling DNA with indolinium compound: To a 1.5 mL of centrifugation vial containing 20 nmole of DNA was added 41.6 μL of 0.1 M sodium phosphate buffer (NaPi), pH 7.8, 41.6 μL of compound 2 in N-methyl 2-pyrrolidone (NMP) (96 mM) and 41.6 μL of NMP. The vial was placed in a shaker and shaked for 4 hr at 37° C. The reaction mixture was desalted by gel filtration using Sephadex G-25 and then purified by reversed-phase C8 column. Indolinium_EDC2 (DNA: SEQ ID NO: 75): 15% yield. LC-MS (negative mode): Calcd for C163H212N57O90P15 (monoisotopic): 1216.7379 [M-5H]−4; Found: 1216.9552 [M-5H]4−; Indolinium_EDC4 (DNA: SEQ ID NO: 77): 22% yield. LC-MS (negative mode): Calcd for C172H221N60O96P15 (monoisotpic): 1280.5002 [M-5H]−4; Found: 1280.7356 [M-5H]−4; Indolinium_EDC5 (DNA: SEQ ID NO: 78): 15% yield. LC-MS (negative mode): Calcd for C166H220N51O95P15 (monoisotpic): 1226.7426 [M-5H]−4; Found: 1226.9657 [M-5H]−4. Indolinium_antizip5 (DNA: SEQ ID NO: 72): 10% yield. LC-MS (negative mode): Calcd for C307H401N108O180P29 (average): 1340.2614 [M-8H]7−; Found: 1340.2705 [M-8H]7−. Indolinium_antizip5m (DNA: SEQ ID NO 71): 10% yield. LC-MS (negative mode): Calcd for C308H404N109O177P29 (monoisotopic): 1336.4969 [M-8H]7−; Found: 1336.673 [M-8H]7− Indolinium_antizip3 (DNA: SEQ ID NO: 70): 5% yield. LC-MS (negative mode): Calcd for C307H404N107O178P29 (monoisotopic): 1332.4034 [M-8H]7−; Found: 1332.6293 [M-8H]7−.
Scheme 4 provides another example of synthesizing DNA conjugated quaternary salt bearing active hydrogen component (benzoindolinium_DNA) following the similar route as indolinium_DNA.
Synthesis of compound 3: (same procedure of synthesizing compound 1): 1,1,2-trimethyl-1H-benzoindole (2.73 g, 13 mmole) and 5-bromovaleric acid (2.36 g, 13 mmole) was heated with rigorous stirring at 110° C. overnight. Total 3.016 g of 4 was obtained after working up as off-white solid (59% yield). 1H NMR (CD3OD) δppm: 8.30 (m), 8.15 (m), 8.05 (d), 7.7 (m), 4.66 (t, 2H), 2.45 (t, 2H), 2.1 (m, 2H), 1.85 (m, 2H), 1.85 (s, 3H), 1.83 (s, 6H). MALDI-MS (positive mode): 310.209.
Synthesis of compound 4: Compound 4 was synthesized following the same procedure of synthesizing compound 2 and was used directly for labeling DNA after ether precipitation.
Labeling DNA with benzoindolinium compound: Following the same procedure of synthesizing indolinium_DNA, total 11.2 nmole of Benzoindolinium_EDC7 (DNA: SEQ ID NO: 79) was obtained starting from 50 nmole of EDC7: 22% yield. LC-MS (negative mode): Calculated for C168H216N56O92P15 + (monoisotopic): 1650.0003 [M-4H]-3; Found: 1650.0359 [M-4H]3−.
Scheme 5 provides one example of synthesizing DNA conjugated aldehyde. The acid functionality in aldehyde precursor is introduced through hydrolysis of a cyano group by hydrogen peroxide (Brady, J. D.; Robins, S. P. J. Bio. Chem. 2001, 276, 18812-18818.).
Synthesis of compound 5: In a 50 mL of round-shaped flask containing N-methyl-N-cyanoethyl-4-aminobenzaldehyde (1.024 g, 5.44 mmole) was added 27.2 mL of 5 N NaOH solution and 6.8 mL of 30% H2O2. The reaction mixture was refluxed for 2 hr. After cooling down, the reaction mixture was neutralized by the addition of concentrated HCl (37% w.t.) and extracted with 2×100 mL of EtOAc and 1×100 mL of CH2Cl2. The organic layers were combined and washed once with 50 mL of brine and concentrated to dryness. The crude product was purified by a 40 g RediSep silica-gel column on a CombiFlash Companion chromatography system (EtOAc/MeOH). Total 0.702 g of light pinkish solid was obtained (62%). Electrospray MS: M+H 208.0735. (Brady, et al., J. Biol. Chem. 2001, 276, 18812-18818).
Labeling DNA with aldehyde: The NHS ester of 5 was synthesized following the same procedure of compound 2. After removing the DCU by filtration, the filtrate was used directly for DNA conjugation (calculated as 0.2 M product in DMF). To a 1.5 mL of centrifugation vial containing 50 nmole of DNA was added 104 μL of 0.1 M NaPi, pH 8.6, 125 μL of the above filtrate and 83 μL of NMP. The vial was placed in a shaker and shaked overnight at 37° C. The reaction mixture was desalted by gel filtration using Sephadex G-25 and then purified by reversed-phase C8 column. Aldehyde_EDC2 (DNA: SEQ ID NO: 75) (44% yield). LC-MS: Calcd for C158H204N57O91P15 (monoisotopic): 1203.9710 [M-4H]−4−; 1605.6306 [M-3H]3− Found: 1203.9664 [M-4H]4−; 1605.6305 [M-3H]3−; Aldehyde_EDC3 (DNA: SEQ ID NO: 76): (49% yield). LC-MS: Calcd for C159H204N59O91P15 (monoisotopic): 1213.9725 [M-4H]4−; 1618.9660 [M-3H]3− Found: 1213.9620 [M-4H]4−; 1618.9590 [M-3H]3. Aldehyde_antizip2 reporter1 (DNA: SEQ ID NO: 69) (30% yield). LC-MS: Calcd for C303H396N110O177P29 (monoisotopic): 1328.2458 [M-7H]7−; Found: 1328.3051 [M-7H]7−.
Scheme 6 provides an example of synthesizing DNA labeled α,β-unsaturated aldehyde 1. Wittig reagent was used for the two-carbon homologation of aldehydes into the corresponding α,β-enals (Eitel, M.; Pindur, U. Synthesis 1989, 364-367. The acid functionality in aldehyde precursor is introduced through hydrolysis of a cyano group by concentrated HCl (Bratenko, M. K.; Chomous, V. A.; Vovk, M. V. Chemistry of Heterocyclic Compounds 2004, 40, 1279-1282).
Synthesis of compound 6: In a 100 mL of round-shaped flask containing N-methyl-N-cyanoethyl-4-aminobenzaldehyde (1.116 g, 5.9 mmole) and ylide (2.71 g, 8.9 mmole) was added 57 mL of dry toluene. The reaction mixture is heated under reflux for overnight, allowed to cool, and filtered through filter paper. After removing the solvent from the filtrate, the residue was first purified by a 40 g RediSep silica-gel column on a CombiFlash Companion chromatography system (Toluene/Ether) and then Preparative HPLC C18 column (Agilent Prep-C18, 30×100 mm, 10 um) to afford 0.27 g of pure product (21%). MALDI-MS (positive mode): 215.226.
Synthesis of compound 7: In a 50 mL of round-shaped flask containing compound 6 (0.1 g, 0.47 mmole) was added 30 mL of concentrated HCl. The reaction mixture was heating to boiling and left at room temperature (RT) for 1 hr. HPLC analysis indicated that only one product was formed and no starting material remained in the reaction mixture. After removing most of the HCl, the compound was dissolved in water and lyophilized to dryness to afford the product.
Labeling DNA with α,β-unsaturated aldehyde: The NHS ester of compound 7 was synthesized following the same procedure as compound 2, however was purified by silica-gel chromatography (EtOAc/Hexanes) instead. After drying under vacuum for several hours, the NHS ester of compound 7 was dissolved in NMP (96 mM) and was used to label DNA following the same procedure as labeling aldehyde_DNA. Aldehyde1_EDC8 (DNA: SEQ ID NO: 80): yield 46%. Calcd for C163H215N48O99P15 (monoisotopic): 1629.9698 [M-3H]−3; Found: 1629.9995 [M-3H]3−. Aldehyde1_antizip2 reporter1 (DNA: SEQ ID NO: 69): yield 40%. Calcd for C305H398N110O177P29 (monoisotopic): 1331.96239 [M-7H]7; Found: 1332.0778 [M-7H]−7.
Example 5 to 8 are related to the preparation of indole and indolinium analogues for DNA conjugation.
Indole analogues can be synthesized following the general Fischer-indole synthesis by converting aryl hydrazones to indoles under acidic conditions (Scheme 7). First, a primary aromatic amine and nitrous acid reacts to give a diazonium salt. The diazonium salt is then reduced to a hydrazine (Hunsberger et. al. J. Org. Chem. 1956, 21, 394-399). Finally hydrazine reacts with 3-methylbutan-2-one to form the aryl hydrazone which upon isomerization and elimination of NH3 forms indole (Lindsey et. al. Tetrahedron 1989, 45, 4845-4866).
To a solution of 4-methoxyaniline (2.46 g, 20 mmol) in 60 mL of conc. HCl was added dropwise the solution of NaNO2 (1.38 g, 20 mmol) in 35 mL of H2O at 0° C. After stirring for 0.5 h at 0° C., the reaction mixture was added dropwise to a solution of SnCl2 (9.03 g, 40 mmol) in 35 mL of conc. HCl at 0° C., then stirring was continued for 1.5 h at 0° C. 2N NaOH was then added to quench the reaction until pH=9 to 10. The aqueous layer was extracted with DCM (50 mL×3) and the organic layer was dried over Na2SO4. After filtration and concentration, the desired product, (4-methoxyphenyl)hydrazine was obtained (0.98 g, 35% yield), which was used directly for next step.
A mixture of (4-methoxyphenyl)hydrazine (0.98 g, 7.1 mmol) and 3-methylbutan-2-one (1.53 g, 17.8 mmol) in 20 mL of HOAc was heated at 100° C. overnight. The mixture was concentrated and 1N NaOH was added until pH 9 to 10. The aqueous solution was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over Na2SO4. After filtration and concentration, the residue was purified by flash column chromatography to give 610 mg of 5-methoxy-2,3,3-trimethyl-3H-indole (45%). 1H NMR (CDCl3) δppm: 7.43 (dd, 1H), 6.81 (m, 2H), 3.83 (s, 3H), 2.26 (s, 3H), 1.28 (s, 6H). LC-MS (M+H): 190.16
(3-nitrophenyl)hydrazine (MW=189.6, 685 mg, 3.6 mmol) and 0.75 ml 3-methyl-2-butanone were stirred in 8 mL of EtOH at RT for 10 minutes, then at 40° C. for 15 minutes. Ethanol was removed under reduced pressure. The residue was taken up in 20 mL of conc. HCl and heated at 100° C. for 2 h. The aq. HCl was then removed under reduced pressure. The solid was triturated with 2 mL of iced water, filtered and washed with 2 mL of iced water. After drying in the air, the solid weighed 300 mg. However, TLC indicated that it contained a mixture of two products. The aqueous layers were neutralized with 1N NaOH to pH˜8.0, extracted with EtOAc (50 mL×3). The organic layers and the solid obtained previously were combined, dried over Na2SO4 overnight. The organic solution was filtered, washed with EtOAc, and concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, 70 g), eluted with 8-15% EtOAc in hexane to give two fractions. The first fraction was obtained in 217 mg (30% yield) as a light yellow oil, which was identified as compound 4-nitro-2,3,3-trimethyl-3H-indole by 1H NMR. 1H NMR (CDCl3) δppm: 8.0 (dd, 1H), 7.89 (dd, 1H), 7.50 (t, 1H), 2.73 (s, 3H), 1.50 (s, 6H). The second fraction was obtained in 245 mg (33% yield) as a yellow solid, which was identified as 6-nitro-2,3,3-trimethyl-3H-inodle by 1H NMR. 1H NMR (CDCl3) δppm: 8.33 (d, 1H), 8.12 (dd, 1H), 7.50 (t, 1H), 7.38 (d, 1H), 2.33 (s, 3H), 1.27 (s, 6H).
A solution of sodium 4-aminonaphthalene-1-sulfonate (2.45 g, 10 mmol) in H2O (15 mL) was added a solution of NaNO2 (0.70 g, 10 mmol) in H2O (2 mL) at 10-15° C. The solution was then added to a cold solution of conc. H2SO4 (0.54 g, 5.5 mmol) in 0.5 mL of H2O. The temperature was maintained below 10° C. and the mixture was stirred for 1.5 h after the addition was complete. The mixture was then added dropwise to a cold solution of SnCl2 (3.8 g, 17 mmol) in 2.5 mL of conc. HCl and 1.5 ml of H2O. The reaction temperature was kept below 10° C. and allowed to sit onemoght. It was filtered and washed thoroughly with H2O. The cake was removed twice from the Buchner funnel and suspended in H2O and filtered. The solid obtained was dried under vacuum to give 1.4 g of 4-hydrazinylnaphthalene-1-sulfonic acid (59%). The material was used directly for next step. A solution of 4-hydrazinylnaphthalene-1-sulfonic acid (0.7 g, 2.9 mmol) in 3 ml of HOAc was added 3-methylbutan-2-one (0.5 ml, 1.5 eq), NaOAc (0.47 g, 2.0 eq.). The mixture was stirred at 110° C. for 3.5 h. After cooling and addition of ether, the precipitate was filtered to give 700 mg. The solid was dissolved in DCM and purified by flash chromatography on SiO2 using 10% MeOH in DCM to give 273 mg of product. The mother liquor was concentrated and was also purified by flash chromatography on silica gel to give additional 372 mg of product. The overall yield was 77%. 1H NMR (DMSO) δppm: 8.8 (dd, 1H), 8.4 (dd, 1H), 8.0 (s, 1H), 7.5 (m, 2H), 3.1 (s, 5H), 2.3 (s, 4H), 1.3 (s, 6H). LC-MS: 288.2 [M−H].
To a solution of 6-aminonaphthalene-2-sulfonic acid (2.23 g, 10 mmol) in 15 ml of H2O was added 2N NaOH (0.75 ml). The mixture was stirred for 5 min at RT and conc. H2SO4 (0.68 g, 6.9 mmol) was added to it dropwise at 0° C. 2 ml of iced H2O was added, followed by a solution of NaNO2 (1.04 g, 15 mmol) in 2 ml of H2O. After the solution was stirred at 0° C. for 2 h, the diazonium salt was removed by filtration and washed with cold water. The salt was then added in portions to a cold (<0° C.) solution of SnCl2 (4.9 g, 22 mmol) in 3.2 ml of conc. HCl and 1.8 ml of H2O. The mixture was stirred overnight. The solid was filtered and washed twice with water, dried under vacuum to give 1.84 g of 6-hydrazinylnaphthalene-2-sulfonic acid (77%), which was used directly for next step.
To a solution of 6-hydrazinylnaphthalene-2-sulfonic acid (0.7 g, 2.9 mmol) in 3 ml of HOAc was added 3-methylbutan-2-one (0.5 ml, 1.5 eq), NaOAc (0.47 g, 2.0 eq.). The mixture was stirred at 110° C. for 3.5 h. After cooling, the solvent was removed under reduced pressure. The residue was dissolved in MeOH and 3.0 g of SiO2 was added. MeOH was removed and the silica gel was loaded on a silica gel column and eluted with 10% MeOH in DCM to give the desired product, 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonic acid (874 mg, >95% yield). LC-MS: 288.2 [M−H]
To a solution of 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonic acid (723 mg, 2.5 mmol) in methanol (5 mL) was added a saturated solution of potassium hydroxide in isopropanol (3.134%, 4.913 g, 1.1 eq.) and the resulting suspension was heated at reflux for 2 h. Then the mixture was concentrated and the corresponding potassium salt was obtained. Under nitrogen atmosphere, a mixture of potassium 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonate and 5-bromovaleric acid (585 mg, 3 mmol) in 3-methyl-2-butanone (5 mL) was heated at 140° C. for 20 h. Removal of the solvent and purification by chromatography (dichloromethane/methanol) afforded 3-(4-carboxybutyl)-1,1,2-trimethyl-1H-benzo[e]indolium-7-sulfonate (70 mg, isolated yield 7.2%). LC-MS: 390.18 [M+].
Scheme 8 provides an example of synthesizing hemicyaine 8 in aqueous buffer in the presence of various catalysts. The extent of hemicyanine formation was easily monitored by analytical reversed-phase HPLC (UV at 545 nm). Hemicyanine 8 has fluorescence excitation wavelength maximum at 535 nm and emission maximum at 580 nm. MALDI-MS analysis of the product confirms the structure (M+: 449.1992). The experimental data indicates (S)-pyrrolidinemethylpyrrolidine ((S)-PMP) has better catalytical ability than other catalysts.
Examples 10-13 are related to DPC of hemicyanine formation.
Scheme 9 gives an example of DPC hemicyanine formation through end of helix architecture. Upon annealing, the two hemicyanine precursors were placed in reactive proximity at the end of helix and a hemicyanine linked to both DNA was formed after condensation.
The progress of DPC reaction was monitored by fluorescence spectroscopy.
DPC reaction: Reactions were performed with 200 nM each of reagent in 10 mM (S)-PMP, 50 mM sodium phosphate buffer, pH 8.4, 1 M NaCl at RT unless otherwise specified. Catalyst (S)-PMP was added after mixing both reagents together in reaction buffer.
Scheme 10 provides another example of DPC hemicyanine formation through middle of helix architecture where the reactants were labeled to two probes which can complementary with a single template. Upon annealing, the two hemicyanine precursors were placed in reactive proximity at the middle of helix and a hemicyanine linked to both DNA was formed. The experimental data indicate only in the presence of the template, fluorescence signal is generated (
DPC reaction: Reactions were performed with 200 nM each of indolinium_EDC5 (DNA: SEQ ID NO: 78), aldehyde_EDC5 (DNA: SEQ ID NO: 78), EDC1 (DNA: SEQ ID NO: 74) in 10 mM (R) —PMP, 50 mM sodium phosphate buffer, pH 8.4, 1M NaCl at RT. (S)-PMP was added after mixing both reagents and template together in the reaction buffer.
The reaction rate for both end-of-helix (Example 10) and middle-of-helix (Example 11) DPC were investigated by fluorescence spectroscopy (
Small molecule hemicyanine dyes (9 to 12) were first synthesized and their fluorescence excitation and emission spectra were recorded (
DPC reaction: Reactions were performed with 200 nM each of strands and template in 10 mM N,N-dimethyl ethylenediamine (DMEDA), 50 mM sodium phosphate buffer, pH 8.4, 150 mM NaCl at RT. Catalyst was added after mixing both reagents and template together in the reaction buffer.
Two hemicyanine products were formed by mixing antizip3_indolinium with antizip2 reporter1_A0 and antizip2 reporter1_A1 respectively (DNA: SEQ ID NO: 69). The product (17) formed between antizip3_indolinium (DNA: SEQ ID NO: 70) and antizip2 reporter1_A0 (DNA: SEQ ID NO: 69) has excitation maximum at 540 nm and emission maximum at 600 nm, while the product (18) formed between antizip3_indolinium (DNA: SEQ ID NO: 70) and antizip2 reporter1_A1 (DNA: SEQ ID NO: 69) had excitation maximum at 600 nm and emission maximum at 670 nm (
DPC reaction: Reactions were performed with 200 nM each of reagent in 15 mM DMEDA, 50 mM sodium phosphate buffer, pH 8.0, 2.5 mM MgCl2 at 30° C. Total reaction volume was 50 μL. Catalyst DMEDA was added after mixing both reagents together in reaction buffer. Fluorescence was recorded immediately after the addition of catalyst DMEDA.
General Examples on Dpc-Based Protein Detection
Five oligonucleotides were prepared using standard phosphoramidite chemistry (Glen Research, Sterling Va., USA). Oligonucleotides bearing 5′-amino groups (Oligo2 and Oligo6) were prepared using 5′-Amino-Modifier 5 and Oligonucleotides bearing 3′-aminogroups (Oligo4 and Oligo5) were prepared using 3′-Amino-Modifier C7 CPG (Glen Research, Sterling Va., USA)
(SEQ. ID. NO. 19)
(SEQ. ID. NO. 20)
(SEQ. ID. NO. 21)
(SEQ. ID. NO. 22)
(SEQ. ID. NO. 23)
Oligo1, Oligo4 and Oligo5 were removed from the synthesis support and purified by reversed-phase HPLC. The amino groups of Oligo2 and Oligo6 were converted while resin-bound to their triphenyl phosphine derivatives and these were purified and isolated (Sakurai et al., J. Amer. Chem. Soc., 2005, 127, pp 1660-1667) to give Oligo2-TPP and Oligo-6TPP, respectively.
Amino group bearing Oligo4 and Oligo5 were converted to their azidocoumarin derivatives (Oligo-4-AzC and Oligo5-AzC, respectively) by reaction of each oligo with the N-hydroxysuccinimide ester of 7-azido-4-methylcoumarin-3-acetic acid (Thevenin et al., Eur. J. Biochem (1992) Vol. 206, pp-471-477). The reaction was performed by adding 1 μL of trifluoroacetic acid to 5 μL of N-methylmorpholine to prepare a buffer to which was added 10 μL of water containing 6.6 nmol of Oligo 4 or Oligo 5, followed by addition of 30 μL of a 0.16 M solution of the coumarin NHS-ester in dimethylformamide. Each reaction was allowed to proceed for 2 hours at room temperature, whereupon 50 μL of 0.1 M aqueous triethylammonium acetate was added. The mixtures were applied to a NAP-5 desalting columns (Amersham Biosciences, Piscataway N.J. USA) and eluted according to the manufacturers instructions the eluate was purified by RP-HPLC to provide Oligo-4-AzC and Oligo5-AzC, in yields of 77% and 70%, respectively. Product identity was confirmed by Maldi-ToF mass spectrometry.
To demonstrate the hybridization-specific creation of fluorescence, various combinations of complementary and non-complementary oligonucleotides bearing azido-coumarin and triphenyl phosphine moieties were allowed to react at room temperature in a buffer comprised of 30% aqueous formamide, 50 mM NaCl, and 10 mM sodium phosphate, pH 7.2. The reaction progress was monitored over time using a Victor Multilabel fluorimeter (EG&G Wallach, Turku Finland) set to excite the sample at 360 nm and monitor light emission at 455 nm
Results of additional experiments involving ternary complexes are shown in
A model system was prepared which included two twenty-mer oligonucleotides with a ten-base complementary region and ten-base single stranded spacer arms, further linked to a six carbon spacer arm. These oligos were synthesized both with and without a 5′-biotin (with a 6-carbon spacer arm). As shown below, the complementary region is underlined. A third oligo was identical to the (−) strand oligo but with 4 base mismatches (italicized) to the (+) strand.
(SEQ. ID. NO. 24)
(SEQ. ID. NO. 25)
(SEQ. ID. NO. 26)
Melting curves of the 10-base pair oligonucleotide pair (oligo 26+oligo 27) were examined by measuring fluorescence of SYBR dye binding to double stranded DNA in a Bio-Rad iCycler (Lipsky, et al., Clinical Chemistry 2001, 47, 635-44). The binding curves are presented as the first derivative of the slope of the melting curve, such that a maximum value represents a point of inflection in the curve (a Tm, or in a mixed population of double stranded sites, a “local” Tm). Binding curves can be obtained up to at least 70° C. as avidin retains biotin binding activity up to this temperature and beyond.
To check the dependence of this particular pair of oligonucleotides upon concentration, melting curves were generated for the oligonucleotide pair varied over the range from 500 to 20 nM (
To test whether binding the (+) and (−) strands to a protein target would cause an increase in Tm, the biotinylated version of these oligonucleotides were incubated in the presence of avidin. Avidin contains 4 equivalent binding sites, which are spaced relatively close together and bind to biotin very tightly (Ka˜<10−15 M) and non-cooperatively.
Presented with equal molar concentrations of oligonucleotides #26 and #27 in biotinylated form, it would be expected that about half of the biotin binding sites are occupied by complementary pairs of oligonucleotides, and about half with the same oligonucleotide (non-complementary pairs). The prediction is that one would observe two melting curve peaks in the presence of avidin. One peak would be the result of any pairs of oligonucleotides which were either not bound to avidin (free in solution) or which had only one partner of the two bound to avidin, which should not exhibit a proximity effect upon Tm. A second peak of significantly higher Tm would represent a pair of biotinylated oligos both bound to avidin, which should exhibit a proximity effect.
Such an experiment was conducted as shown in
Results were essentially identical if the experiment was conducted by adding equimolar amounts of both the oligonucleotides at room temperature, ramping to 60° C., and then obtaining the melting curves. In this method (as well as the hot start method) suitable melting curves can be generated by adding an excess molar of each oligo relative to avidin if desired. (Large excesses of pairs of oligos increases the size of the low Tm peak, however, as predicted.) This was not detrimental in forming high Tm hybrid DNA since the pairs of oligos competed equally for biotin binding sites as long as they were added together in equal molar amounts. If oligos were added one at a time, it was important to add about a 2:1 molar ratio of the first oligo to avidin followed by a 2:1 ratio of the second oligo. With sequential addition, adding an excess molar amount of either oligo relative to avidin occupies all the binding sites of the avidin with the first oligo and prevents occupying adjacent sites with the second, complementary oligo and exhibiting the elevated Tm effect. These observations are consistent with the mechanism being binding of adjacent pairs of complementary oligos to two adjacent biotin binding sites to obtain hybrids exhibiting the elevated Tm peaks.
Experiments were also conducted with a 10-base self-complementary oligonucleotide which was composed entirely of A and T. (Oligo 31: 5′-biotin-spacer arm-TTTTTTTTTTTTTAATTAAA) (SEQ. ID. NO. 27). Because this oligonucleotide was homogeneous in base composition and composed entirely of AT, it melted at a lower Tm than the above-described model system and produced a fairly sharp melting curve. In the presence of avidin, its Tm was increased from 30.5° C. to 61.5° C. (
These experiments were repeated using anti-biotin antibody as a target rather than avidin. Anti-biotin antibody contains two biotin binding sites located near the ends of the Fab portion of the antibody, but the binding sites are much further apart than the biotin binding sites on avidin.
Here, an exemplary system was designed to utilize nucleic acid-templated azidocoumarin (AzC)-triphenylphosphine (TPP) chemistry to detect a protein target upon aptamer binding and annealing of the two complementary DNA probes.
Human PDGF-BB and PDGF-AA was obtained from R&D Systems (220-BB and 220-AA, respectively). Anti-human PDGF-B Subunit monoclonal antibody was obtained from R&D Systems (MAB2201). Buffers included Tris/Mg buffer, at 50 mM Tris/HCl, pH 8.0-10 mM MgCl2. Oligonucleotides used were as follows:
Oligonucleotide Sequences Used in this Example
Oligo #/ 5′- 3′- (SEQ. Mod′ Mod Descrip- ID #) Sequence (5′ to 3′) f. ′f. tion 201 CAGGCTACGGCACGTAGAGCATCACC TPP none DPC- (28) ATGATCCTGCCCCCCCCCCATATTTA aptamer AGC probe 202 GCTTAAATATCCCCCCCCCCCAGGCT none AZC DPC- (29) ACGGCACGTAGAGCATCACCATGATC aptamer CTG probe 203 GTGGGAATGGTGCCCCCCCCCCCAGG none AZC DPC- (30) CTACGGCACGTAGAGCATCACCATGA aptamer TCCTG probe- mismatch 204 GTGGTAGTTGGAGTCGTGGCGTAGGC none none target (31) AAGA 205 GTGGTAGTTGGAGTCACACGTGGCGT none none target (32) AGGCAAGA 206 GTGGTAGTTGGAGCTCACACCACACG none none target (33) TGGCGTAGGCAAGA 207 GTGGTAGTTGGAGTCACACACACCAC none none target (34) ACACAGTGGCGTAGGCAAGA 208 GTGGTAGTTGGAGCTCACACCACACC none none target (35) AACCACACCACACCACACACACCACA CGTGGCGTAGGCAAGA 209 GTGTGGTGTGGTGTGGTGTG none none splint (36) 210 GTGGCGTAGGCAAGAGTGGTAGTTGG none none K-ras (37) AGCT target outward facing 211 GTGGGAATGGTG none TPP TPP (38) probe 212 AGATCCCACTAGCAC TPP none TPP (39) probe 213 AGCTCCAACTACCAC TPP none TPP (40) “mis- match” 214 TCTTGCCTACGCCAC none AZC AZC (41) probe 215 CAGGCTACGGCACGTAGAGCATCACC none none aptamer (42) ATGATCCTG
DPC Reaction conditions. Except as noted, each 100 microliter reaction contained, in a total volume of 100 μl, 1×Tris/Mg buffer, 40 picomoles of TPP and AzC reaction probes, 40 picomoles of target oligonucleotide or of target protein, and typically 25-30% v/v of formamide. Samples were incubated at 25° C. in a Wallac Victor 1420 spectrophotometer and the increase in fluorescence monitored with excitation at 355 nm and emission at 460 nm.
Results: Detection of PDGF-BB by Aptamer-DPC Probes
As illustrated in
As shown in
The DNA-dependence of the reaction was critically dependent upon the melting temperature of the DNA relative to the assay temperature. In the presence of 0% formamide (with the calculated and observed Tm>Tassay, the reaction took place in the presence or absence of the target protein PDGF-BB (
DNA melting experiments with the complementary sequences, monitored with SYBR Green had indicated a Tm of the sequence of about 30° C. in the Tris/Mg buffer in the absence of formamide, and about 7° C. lower for every 10% increase in formamide. Tm in the optimal formamide concentration for the detection assay, 30%, was 10° C.
In 0% formamide, the oligonucleotides can form at least a partial duplex even in the absence of PDGF-BB (Tm slightly higher than Tassay). The DNA target-dependence of the reactions in 20% and 30% formamide is explained by the assay being conducted at a temperature greater than the Tm in the absence of protein target. No reaction occurs unless the Tm of the complex is increased by the binding of the two probes to the PDGF-BB target. At 40% formamide, the reaction doesn't occur with any set of reactions. The likely explanation is that either the Tm had been reduced so low that binding to PDGF-BB could not raise it above Tassay, or that formamide had inhibited PDGF-BB binding to the aptamers. A more complex situation is the observed inhibition of reaction rate upon addition of PDGF-BB in the absence of formamide. Since half of the duplexes formed by PDGF-BB are non-productive (50% will be homoduplexes) the reduction in rate is likely due to PDGF-BB binding preventing these homoduplexes from disassociating and then reassociating in solution with complementary pairs to form heteroduplexes. This situation should not occur using pairs of probes specifically directed against different binding sites in a heterodimeric target.
The sensitivity of the assay (
The assay sensitivity was also determined using PDGF-AA as a target. The aptamer monomer is expected to have an affinity for PDGF-AA about ten times weaker than for PDGF-BB. However, since the assay involves forming a complex of two aptamer-dimers to either type of PDGF, the avidity of binding of the dimer is expected to be tighter than the affinity of the monomer, and its affinity should be substantially tighter (lower Ki) than the concentrations tested of the target PDGFs (down to about 1 nanomolar). As shown in
Ratios of TPP to AzC Probes. To confirm the model of the reaction mechanism (
Thus, in this model system fluorescence was not generated unless the aptamers bound and the complementary sequences in the two probes annealed to each other.
The reaction, in 35% formamide at 22° C., was dependent upon the presence of both of the reporter oligonucleotides, both of the aptamer oligonucleotides, and the target, PDGF-BB (
Confirmation of the correctness of the model was obtained with experiments varying the ratio of the TPP and AzC aptamer oligos (
These experiments indicate that the complex can self-assemble in solution, such that each zip code and its anti-zip code anneal to each other with minimal interference with the aptamer sequence or the reporter sequences.
Experiments were also conducted to determine if the order of addition, and thus assembly of the aptamer and reporter probes, was of any importance. Slightly slower reaction rates were obtained if the aptamer oligonucleotides were first incubated with PDGF before adding the reporter oligonucleotides, compared with adding all probes together as a mixture. Somewhat greater reaction rates were obtained if each pair of aptamer oligonucleotides and reporter oligonucleotides was first incubated and allowed to assemble with each other before the two sets were mixed together and incubated with PDGF. The reason for this may be that there is some steric hindrance to zip code-anti zip code annealing to aptamer probe if the aptamer probe is already bound to target.
As a control, a set of one-piece TPP and AzC probes was compared which contained only the zip code sequences and no zip code-anti zip code sequences (
The sequence of the aptamer-containing TPP and AzC probes was also systematically varied to determine any constraints on the design. The aptamer-containing TPP and AzC oligos were synthesized, both having the same sequences as described in
Oligonucleotides used in this example included:
(SEQ. ID NO. 43)
X = C18 PEG;
AZC = 3′-AzC.
(SEQ. ID NO. 44)
X = C18 PEG,
(SEQ. ID NO. 45)
X = C18 PEG
(SEQ. ID NO. 46)
X = C18 PEG
(SEQ. ID NO. 47)
(SEQ. ID NO. 48)
(SEQ. ID NO. 49)
(SEQ. ID NO. 50)
(SEQ. ID NO. 51)
(SEQ. ID NO. 52)
(SEQ. ID NO. 53)
(SEQ. ID NO. 54)
(SEQ. ID NO. 55)
(SEQ. ID NO. 56)
None of these changes resulted in a significant difference in the performance of the system. Experiments 4) and 5) also resulted in a 3 and 6-base single stranded (not annealed to zip code) structure immediately upstream of the C18 spacer in the reporter oligonucleotides.
The results of these experiments indicate that the aptamer-based PDGF detection system can be assembled separating the binding and DPC functions into two separate oligonucleotides. Through the selection of appropriate zip code sequences, the detection format described in
These results indicate that a zip-coded reporting approach can be effectively designed, for example, using aptamer-containing oligonucleotides.
While the results with the aptamer system indicate that a stable complex between binding and reporter sequences can be formed simply by annealing the zip code and anti-zip code regions, it should be noted that there are technologies to covalently and irreversibly link the two oligonucleotides together, with a high likelihood of retaining activity of the reporter reactive groups. For example, the oligonucleotides may be incubated in pairs (a binder oligonucleotide and a reactive oligonucleotide for nucleic acid-template chemistry) at a temperature at which the zip codes and anti-zip codes are mostly double stranded, but the rest of the sequences are single-stranded. Adding an intercalating, photoactivatable cross-linker such as Trioxalen, followed by UV irradiation, may irreversibly crosslink the two strands. Similarly, UV irradiation may introduce thymidine dimers between separate strands of annealed sequences. Alternately, a sequence may be introduced complementary to a short target (splice) DNA, abutting 3′ and 5′, which may then be ligated with DNA ligase. The splice oligonucleotide may alternately be composed of RNA, and removed after ligation with RNase H, which hydrolyzes RNA annealed to DNA. This can result in converting the two oligonucleotides into a single piece of single-stranded DNA. These methods can lead to cost-effective production of oligonucleotide reagents in detection kits against specific targets.
Relevant references for this example include Capaldi, et al., Nucleic Acid Res. 2000, 28, e21.; Castiglioni, et al., Appl. and Exper. Microbio. 2004, 7161-72; Fang, et al., Chem. BioChem. 2003, 4, 829-34.; Gerry, et al., J. Mol. Biol. 1999, 292, 251-62.
In another embodiment, the aptamer sequences are replaced with non-DNA binders such as antibodies. For PDGF and other protein targets, the aptamer sequences are replaced with chemically active groups, such as aldehydes, and reacted with non-DNA binder sequences such as antibodies or receptors to the protein targets (
The SoluLink technology for conjugation of the antibody and oligonucleotides first requires modification of the primary amino groups of the antibody with succinimidyl 2-hydrazinonicotinate acetone hydrazone) to incorporate an acetone hydrazone onto the antibody. The primary amines of the oligonucleotides are separately activated with succinimidyl 4-formylbenzoate. The two activated molecules are mixed in the desired ratio (typically 6:1) and reacted at a mildly acidic pH to form a stable hydrazone linkage. The details of this chemistry are available at www.SoluLink.com. Two conjugates were prepared: one containing the zip code to anneal to the AzC-containing reporter oligonucleotide, and the other containing the zip code to anneal to the TPP-containing reporter oligonucleotide.
The antibody-oligonucleotide conjugates received from SoluLink were further purified by gel chromatography on a 1.6×60 cm column of Superdex S-200 (Amersham Biosciences) in PBS buffer (0.01 M potassium phosphate, pH 7.4-0.138 M sodium chloride). The main antibody peak, eluting at about 0.6 times the column volume, was collected and a later eluting peak of contaminating non-conjugated oligonucleotide was discarded. The antibody conjugate was concentrated by reversed dialysis with a Pierce (Rockford, Ill.) 30 K molecular weight cut-off Slide-A-Lyzer using Pierce Concentrating Solution. The protein content was determined using the Bio-Rad Micro BCA Reagent Kit and the oligonucleotide content determined using SYBR Gold DNA binding dye (Molecular Probes (Eugene, Oreg.). The conjugates were both determined to contain an average of approximately 3 oligonucleotides per protein molecule.
Recombinant human PDGF-BB (220-BB) and mouse monoclonal anti-PDGF-BB (MAB220) were obtained from R&D Systems (Minneapolis Minn.).
Sequences used in this study included (where AzC indicates azidocoumarin and TPP indicates triphenylphosphine):
TPP-(amino modifier C6)-CGAATTTATA-C18PEG-TCAGCATCGTACCTCAGC
(SEQ ID NO.: 9) (SEQ ID NO.: 58)
GGACTCGAGCACCAATAC-C18 PEG-TATAAATTCG-(amino modifier C7)-AzC
(SEQ ID NO.: 14) (SEQ ID NO.: 10)
AzC zip code
TTGGTGCTCGAGTCCCCCCCCCCCCCCCCCCCCCC-(amino modifier C7)
(SEQ ID NO.: 59)
TPP zip code
(amino modifier C6)-CCCCCCCCCCCCCCCCCCCCGCTGAGGTACGATGCTGA
(SEQ ID NO.: 60)
In addition, the 5′ amino modifier C6 was obtained from Glen Research (from Glen Research phosphoramidite 110-1906). The 3′-amino modifier C7 was obtained from Glen Research (from Glen Research CPG 20-2957). The C18 PEG was obtained from Glen Research (from Glen Research phosphoramidite 10-1918).
Assembly of Antibody-oligo Conjugates with Reporter Oligonucleotides.
The two antibody-oligo conjugates with their reporter were first assembled separately in a volume of 10 μl. Each assembly contained 0.5 μM (5 picomoles) of antibody-oligonucleotide conjugate and 0.15 μM of (15 pmoles) of complementary reporter oligonucleotide in 0.05 M Tris/HCl pH 8-0.01 M magnesium chloride. Each was incubated for at least 15 minutes at 4° C. before use in the detection reaction mixture.
Detection Reaction of Anti-PDGF-BB DPC Conjugates/Reporters with PDGF-BB
To conduct detection reaction, each reaction may contain in a volume of 50 μl: 10 μl of each conjugate assembly, prepared as described above, and variable amounts of PDGF-BB, in a buffer of 0.05 M Tris/HCl pH 8-0.01 M magnesium chloride-40% volume/volume formamide. The conjugates are present in this reaction mixture at 0.2 μM. Samples are incubated in the wells of a black 96-well microplate in a Wallac Victor Luminometer at 25° C. Fluorescence can be followed vs. time with excitation at 355 nm and emission at 460 nm.
Reactions typically may be carried out at 25° C., monitoring fluorescence generation at the wavelength optimums of the reaction product, 7-amino coumarin.
The entire disclosure of each of the publications and patent documents referred to herein is incorporated by reference in its entirety for all purposes to the same extent as if each individual publication or patent document were so individually denoted.
The invention may be embodied in other specific forms without departing form the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting on the invention described herein. Scope of the invention is thus indicated by the appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein.
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|U.S. Classification||436/86, 562/433, 548/510, 436/94, 436/96, 548/427, 536/23.1, 548/544, 548/467|
|International Classification||G01N33/68, C07H21/04, G01N33/00, C07C229/40, C07D207/46, C07D209/56, C07D209/04|
|Cooperative Classification||C09B23/105, Y10T436/145555, G01N33/533, C07D209/58, Y10T436/143333, C07D209/08, C09B23/0091, C07D209/56, C07D209/14, C07H21/04, G01N33/5308|
|European Classification||G01N33/53F, C07D209/14, C09B23/00S, C07D209/08, C07H21/04, C07D209/58, C07D209/56, G01N33/533|
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